1,3,5-TRI-O-ACETYL-2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSE
1,3,5-Tri-O-acetyl-2-deoxy-beta-D-erythro-pentofuranose
CAS: 96291-75-7
Molecular Formula: C11H16O7
1,3,5-TRI-O-ACETYL-2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSE - Names and Identifiers
| Name | 1,3,5-Tri-O-acetyl-2-deoxy-beta-D-erythro-pentofuranose |
| Synonyms | B-D-ERYTHRO-PENTOFURANOSE 1,3,5-Tri-O-acetyl-2-deoxy-b-D-ribofuranose b-D-erythro-Pentofuranose,2-deoxy-, 1,3,5-triacetate 1,3,5-Tri-O-acetyl-2-deoxy-beta-D-erythro-pentofuranose 1,3,5-TRI-O-ACETYL-2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSE (2S,4S,5R)-5-(Acetoxymethyl)tetrahydrofuran-2,4-diyl diacetate |
| CAS | 96291-75-7 |
| InChI | InChI=1/C11H16O7/c1-6(12)15-5-10-9(16-7(2)13)4-11(18-10)17-8(3)14/h9-11H,4-5H2,1-3H3/t9-,10+,11+/m0/s1 |
1,3,5-TRI-O-ACETYL-2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSE - Physico-chemical Properties
| Molecular Formula | C11H16O7 |
| Molar Mass | 260.24 |
| Density | 1.24±0.1 g/cm3(Predicted) |
| Boling Point | 329.3±42.0 °C(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.466 |
1,3,5-TRI-O-ACETYL-2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSE - Introduction
1,3, is an organic compound whose chemical formula is C12H16O7. It is a deoxygenated furanose (pentofuranose) with acetyl groups at the 3 and 5 positions.
The compound is often used as an important intermediate in organic synthesis, especially plays a key role in the synthesis of carbohydrates. Its main uses include as an important raw material for drug synthesis, as a reagent for organic synthesis, and for sugar chemistry research.
There are a variety of methods for preparing 1,3. One common synthetic method is by deprotection (deprotection) reactions. First, acetyl groups were introduced at positions 3 and 5 to form an acetyl-protected pentofuranose (protected pentofuranose). Then, the acetyl protecting group is removed by appropriate reaction conditions to obtain the target product.
For safety information, 1,3, refer to the relevant chemical literature and manufacturer's safety data sheets for specific properties and safety data. To use the compound, follow laboratory safety practices and take the necessary precautions, including wearing goggles, gloves and laboratory clothing, and operating in a well-ventilated environment. At the same time, follow the relevant laws and regulations, the correct disposal of waste items.
The compound is often used as an important intermediate in organic synthesis, especially plays a key role in the synthesis of carbohydrates. Its main uses include as an important raw material for drug synthesis, as a reagent for organic synthesis, and for sugar chemistry research.
There are a variety of methods for preparing 1,3. One common synthetic method is by deprotection (deprotection) reactions. First, acetyl groups were introduced at positions 3 and 5 to form an acetyl-protected pentofuranose (protected pentofuranose). Then, the acetyl protecting group is removed by appropriate reaction conditions to obtain the target product.
For safety information, 1,3, refer to the relevant chemical literature and manufacturer's safety data sheets for specific properties and safety data. To use the compound, follow laboratory safety practices and take the necessary precautions, including wearing goggles, gloves and laboratory clothing, and operating in a well-ventilated environment. At the same time, follow the relevant laws and regulations, the correct disposal of waste items.
Last Update：2024-04-09 21:11:58
